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QC technician Leiden Oxford Global Resources

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Gevraagd

  • Fulltime
  • Engels (taal)

Aanbod

  • Loondienst (vast)
  • Overdag/avond
 

Vacature in het kort

Leiden
Join a dynamic team as a Quality Control Technician, supporting impactful therapeutic development with a focus on analytical and microbiological testing for integrity and GMP compliance. Engage in method validation, equipment maintenance, and enjoy a collaborative international work environment. Participate in continuous improvement while gaining exposure to cutting-edge techniques like Flow Cytometry, ELISA, and PCR. Contribute to medical breakthroughs within a progressive company culture. Read on to discover why this challenge awaits you.
 

Over het bedrijf

Oxford Global Resources
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Volledige vacaturetekst

We are looking for QC technicians to join one of our clients in the pharmaceutical industry.

About the Client
Our client is a leading pharmaceutical company based in the Leiden region, recognized for its commitment to advancing healthcare through innovation and scientific excellence. With a strong focus on developing and delivering high-impact therapies, the company operates at the intersection of cutting-edge research and patient-centered care. Their collaborative work environment and international team make it an ideal place for professionals seeking to contribute to meaningful medical breakthroughs.

Job Description
We are seeking a Quality Control Technician to join a fast-paced and highly collaborative team. This role involves performing analytical and microbiological testing to ensure product integrity and compliance with GMP standards. The technician will support various laboratory functions including method validation, equipment maintenance, and documentation. The position is based near Leiden and offers exposure to cutting-edge therapeutic development.

Responsibilities

  • Conduct routine testing of products, raw materials, and environmental samples
  • Work in shifts (morning and evening)
  • Execute analytical techniques such as Flow Cytometry, ELISA, and PCR
  • Support method transfer, validation, and qualification activities
  • Maintain and troubleshoot laboratory instruments
  • Ensure compliance with GMP standards and contribute to lab efficiency
  • Participate in investigations and continuous improvement initiatives
  • Manage inventory of critical reagents and consumables
  • Draft and update SOPs and work instructions

Requirements

  • Bachelor's or Master's degree in Life Sciences, Biotechnology, or related field
  • 1-3 years of experience in a GMP-regulated QC laboratory
  • Proficiency in Flow Cytometry, cell-based assays, and PCR techniques
  • Familiarity with microbiological testing methods is a plus
  • Strong communication and documentation skills
  • Proactive mindset with the ability to adapt to shifting priorities
  • Comfortable working in a dynamic, multi-disciplinary lab environment
  • Fluent in English; additional languages are a bonus

Reference: 26617

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